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1416323-25-5

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1416323-25-5 Usage

General Description

3-(4-Methoxyphenyl)oxetane-3-carboxylic acid is a chemical compound with a molecular formula C11H12O4. It is an oxetane derivative with a carboxylic acid functional group and a 4-methoxyphenyl substituent. Oxetanes are cyclic ethers with a four-membered ring structure, and they have been found to have various biological and pharmaceutical applications. The presence of the methoxy group in the phenyl ring may contribute to its properties and potential uses. 3-(4-Methoxyphenyl)oxetane-3-carboxylic acid may have applications in drug development, materials science, and organic synthesis due to its unique structure and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 1416323-25-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,3,2 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1416323-25:
(9*1)+(8*4)+(7*1)+(6*6)+(5*3)+(4*2)+(3*3)+(2*2)+(1*5)=125
125 % 10 = 5
So 1416323-25-5 is a valid CAS Registry Number.

1416323-25-5Downstream Products

1416323-25-5Relevant articles and documents

Preparation method and application of 3-(substituted phenyl) oxetane-3-carboxylic acid and intermediate thereof

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, (2020/11/12)

The preparation method comprises the following steps: taking 3-oxetanone (compound II) as an initial raw material, and carrying out Wittig reaction on the initial raw material and triethyl phosphonotriacetate under an alkaline condition to obtain a compound III; carrying out coupling reaction on the compound III and a boric acid compound IV to obtain a compound V; reducing the ester group of the compound V to generate a compound VI; carrying out nucleophilic substitution reaction on hydroxyl of the compound VI and sulfonyl chloride/sulfonic anhydride to generate a compound VII; reacting hydroxyl of the compound VI with a halogenating reagent to generate a compound VIII; carrying out elimination reaction on the compound VII or the compound VIII to generate a compound IX; and finally, oxidizing the double bonds of the compound IX to generate 3-(substituted phenyl) oxetane-3-carboxylic acid (compound I). The method is easy and convenient to operate and high in yield, the total yield can reach 35%, and large-scale production can be achieved.

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